increased prepulse inhibition Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the ability of a relatively mild stimulus to suppress the response to a strong, startle-eliciting stimulus (Mammalian Phenotype Ontology, MP_0009141)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009141
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Genes

17 gene mutations causing the increased prepulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CIB2 calcium and integrin binding family member 2
ELMOD1 ELMO/CED-12 domain containing 1
FMR1 fragile X mental retardation 1
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GRID2 glutamate receptor, ionotropic, delta 2
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
GRM4 glutamate receptor, metabotropic 4
HTR1F 5-hydroxytryptamine (serotonin) receptor 1F, G protein-coupled
IMPA2 inositol(myo)-1(or 4)-monophosphatase 2
KDM8 lysine (K)-specific demethylase 8
MPI mannose phosphate isomerase
NPTN neuroplastin
NTSR2 neurotensin receptor 2
RNF103 ring finger protein 103
SCN9A sodium channel, voltage gated, type IX alpha subunit
SEPT5 septin 5
SETMAR SET domain and mariner transposase fusion gene